Foam materials with controllable pore structure prepared from nanofibrillated cellulose with addition of alcohols

Low-density foams based on nanofibrillated cellulose (NFC) made from Pinus massonianesoftwood pulp were prepared from NFC aqueous suspensions containing one of four C2–C4alcohols followed by freeze-drying, with the goal of controlling their pore structure and reducing the shrink rate. The foams prepared from NFC suspensions containing ethanol, isopropanol and n-butanol exhibited highly porous structures with a honeycomb-like cellular texture featuring well-defined “cell walls” between the layers. By contrast, the tert-butanol/NFC foam featured a higher number of smaller size pores with irregular shape. The foams prepared by freezing at −196 °C with ethanol also revealed small size pores, with no layered pore structure. The results obtained suggested that freeze-drying could be used to control the key foam parameters by adding different alcohols into an NFC suspension and adjusting the freezing temperature. Combining the obtained information, a possible formation mechanism was proposed. The microstructure, density, porosity, shrinkage, mechanical properties and thermal properties of NFC foams were determined. The obtained NFC foams feature low shrinkage upon formation and thermal conductivity. Smaller Young’s modulus and energy absorption yet similar yield stress values compared to the blank indicate that the freeze-drying in the presence of alcohols tends to generate “soft” foams

Effects of acid hydrolysis waste liquid recycle on preparation of microcrystalline cellulose

Large amounts of acidic waste are produced on the industrial scale during hydrolysis of partially amorphous cellulose to produce microcrystalline cellulose (MCC). The essential disposal and treatment of this highly acidic liquid wastes the acid feedstock and increases the production cost. To maximize the use of acid without sacrificing the MCC product quality, this project reports a successful attempt to recycle the acid hydrolysis waste liquid, focusing on the impact of waste recycling on MCC morphology and reducing sugar in the hydrolysate. The results showed that when the waste liquid is recycled 1-5 times, no metal accumulation occurred while cellulose particles remained intact, maintaining their shape and size. Their extent of crystallinity remained nearly constant, even increasing slightly with up to three cycles. The concentration of reducing sugar showed growth when recycling the waste liquid up to three times, although not quite to the levels that would allow for its cost-effective fermentation. The acid amount to be added at the start of each cycle was near 50% of that used on the first stage

Optimization of Selective Acid Hydrolysis of Cellulose for Microcrystalline Cellulose using FeCl3

In the process of acid hydrolysis of cellulose, hydrolyzing the amorphous regions while retaining the crystalline regions is the key technology for obtaining microcrystalline cellulose products. This paper investigated the influence of FeCl3 on selective acid hydrolysis of crystalline regions and amorphous regions of cellulose. X-ray diffraction data indicated that FeCl3 can enhance the selectivity of acid hydrolysis for amorphous regions of cellulose, thus improving the crystallinity of hydrocellulose. Meanwhile, the crystalline structure did not change. Response surface methodology (RSM) was employed to optimize the crystallinity of hydrocellulose with respect to FeCl3 concentration, HCl concentration, reaction time, and temperature, and the relevant mathematical regression equation model was established. Under optimal conditions, the crystallinity of hydrocellulose was as high as 63.59% at 88.28 °C, 2.46 M HCl, 0.4 M FeCl3, and reaction duration of 64.02 min, which was in agreement with the predicted value

TiO₂-Coated Silicon Nanoparticle Core-Shell Structure for High-Capacity Lithium-Ion Battery Anode Materials

Silicon-based anode materials are considered one of the highly promising anode materials due to their high theoretical energy density; however, problems such as volume effects and solid electrolyte interface film (SEI) instability limit the practical applications. Herein, silicon nanoparticles (SiNPs) are used as the nucleus and anatase titanium dioxide (TiO2) is used as the buffer layer to form a core-shell structure to adapt to the volume change of the silicon-based material and improve the overall interfacial stability of the electrode. In addition, silver nanowires (AgNWs) doping makes it possible to form a conductive network structure to improve the conductivity of the material. We used the core-shell structure SiNPs@TiO2/AgNWs composite as an anode material for high-efficiency Li-ion batteries. Compared with the pure SiNPs electrode, the SiNPs@TiO2/AgNWs electrode exhibits excellent electrochemical performance with a first discharge specific capacity of 3524.2 mAh·g−1 at a current density of 400 mA·g−1, which provides a new idea for the preparation of silicon-based anode materials for high-performance lithium-ion batteries

Effects of acid hydrolysis waste liquid recycle on preparation of microcrystalline cellulose

Large amounts of acidic waste are produced on the industrial scale during hydrolysis of partially amorphous cellulose to produce microcrystalline cellulose (MCC). The essential disposal and treatment of this highly acidic liquid wastes the acid feedstock and increases the production cost. To maximize the use of acid without sacrificing the MCC product quality, this project reports a successful attempt to recycle the acid hydrolysis waste liquid, focusing on the impact of waste recycling on MCC morphology and reducing sugar in the hydrolysate. The results showed that when the waste liquid is recycled 1-5 times, no metal accumulation occurred while cellulose particles remained intact, maintaining their shape and size. Their extent of crystallinity remained nearly constant, even increasing slightly with up to three cycles. The concentration of reducing sugar showed growth when recycling the waste liquid up to three times, although not quite to the levels that would allow for its cost-effective fermentation. The acid amount to be added at the start of each cycle was near 50% of that used on the first stage

Interaction of TAGLN and USP1 promotes ZEB1 ubiquitination degradation in UV-induced skin photoaging

Abstract Background Ultraviolet A (UVA) irradiation can lead to skin damage and premature skin aging known as photoaging. This work found that UVA irradiation caused an imbalance between dermal matrix synthesis and degradation through the aberrant upregulation of transgelin (TAGLN) and studied the underlying molecular mechanism. Results Co-immunoprecipitation and proximal ligation assay results showed that TAGLN can interact with USP1. USP1 can be retained in the cytoplasm by TAGLN in UVA-induced cells, which inhibits the interaction between USP1/zinc finger E-box binding homeobox 1 (ZEB1), promote the ubiquitination degradation of ZEB1, and lead to photoaging. TAGLN knockdown can release USP1 retention and help human skin fibroblasts (HSFs) resist UVA-induced damage. The interactive interface inhibitors of TAGLN/USP1 were screened via virtual docking to search for small molecules that inhibit photoaging. Zerumbone (Zer), a natural product isolated from Zingiber zerumbet (L.) Smith, was screened out. Zer can competitively bind TAGLN to reduce the retention of USP1 in the cytoplasm and the degradation of ZEB1 ubiquitination in UV-induced HSFs. The poor solubility and permeability of Zer can be improved by preparing it as a nanoemulsion, which can effectively prevent skin photoaging caused by UVA in wild-type (WT) mice. Zer cannot effectively resist the photoaging caused by UVA in Tagln −/− mice because of target loss. Conclusions The present results showed that the interaction of TAGLN and USP1 can promote ZEB1 ubiquitination degradation in UV-induced skin photoaging, and Zer can be used as an interactive interface inhibitor of TAGLN/USP1 to prevent photoaging

High Strength Magnetic/Temperature Dual-Response Hydrogels for Applications as Actuators

Anisotropically structured magnetic/temperature dual-response hydrogels have great application prospects as actuators because they can exhibit controlled, complex behaviors. However, one key issue hindering the application of such hydrogels is the imbalance of the mechanical and response properties. This study used a combination of flexible chain polymers such as poly(N-isopropylacrylamide) (PNIPAM), poly(vinyl alcohol) (PVA), and polyacrylamide (PAM) to build a multinetwork structure. The introduction of TEMPO-oxidized cellulose nanofibrils (TOCNF) as a nanofiber reinforcement agent led to a key improvement to ensure a high mechanical strength by creating additional hydrogen bonding. The cross-linking density was further increased through a salting out treatment to obtain a greater mechanical strength while improving the dissipation of energy applied by external sources. The obtained temperature responsive layer featured a high tensile strength (1.97 MPa) while the magnetically responsive layer showed a high magnetization (6.1 emu/g) with a good tensile strength (0.47 MPa). The main idea of this study was in combining two hydrogel layers with different polymer network structures, with magnetic nanoparticles being dispersed within one layer, whereas the other layer was designed as temperature-sensitive. The obtained bilayer hydrogel had suitable mechanical properties (the tensile strength reaching 0.81 MPa) coupled with strong dissipation of the applied external energy and could rapidly and reversibly undergo bending deformations upon a temperature change within a narrow range, 25–37 °C (bending angle up to 160° within 5 min). With high magnetization characteristics for the magnetically responsive layer, the bilayer hydrogel could easily be driven by an external magnetic field to transport a target object, which was “grabbed” due to the gel bending. It also showed good biocompatibility, thus enabling applications in the field of invasive medical actuators

Rechallenge of immune checkpoint inhibitors in advanced non‐small cell lung cancer

Abstract Immune checkpoint inhibitor (ICI) rechallenge in non‐small cell lung cancer (NSCLC) is a promising therapeutic strategy. The situation for ICI rechallenge can be divided into three categories: adverse events (AEs); resistance to ICIs, and rechallenge becomes compulsive because of tumor relapse while the patients had completed a 2 year course of immunotherapy. However, these categories are still controversial and should be explored further. Through voting at the 6th Straits Summit Forum on Lung Cancer, in this study we summarize the consensus of 147 experts in ICI rechallenges. A total of 97.74% experts agreed to rechallenge; 48.87% experts rechallenge with the original drug, and the others rechallenge with a different drug; 40.3% agreed to rechallenge directly after progression; 88.06% experts agreed to ICI rechallenge with a combination regimen; and factors such as previous performance status score, PD‐1 expression, and age should also be considered. Understanding the the clinical studies in ICI rechallenge could bring us one step closer to understanding the consensus. In patients with advanced NSCLC who have suffered recurrent or distant metastasis after immunotherapy, the option of rechallenge with ICIs is a promising treatment option